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Noxopharm

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uuid0005uce

Namestring
Noxopharm
Legal namestring
Noxopharm Limited
Websiteurl
noxopharm.com
Company typeenum
Public
Founded yearint
2015
Descriptiontext

Noxopharm Limited (ASX:NOX) is an Australian clinical-stage biotechnology company founded in 2015 and headquartered in Castle Hill, NSW, developing novel therapeutics across oncology, autoimmune/inflammatory disease, and mRNA vaccine enhancement. The company operates two proprietary technology platforms: Sofra™, an oligonucleotide-based platform using short nucleic acid sequences to amplify Toll-like receptor 8 (TLR8) activity, which the company reports achieves more than 200-fold activity improvement over current best-in-class clinical comparators in human skin biopsies; and Chroma™, a small-molecule platform generating multiple oncology drug candidates, with leading preclinical asset CRO-67 positioned for pancreatic cancer.

The company's clinical pipeline centres on Veyonda®, which is in a Phase 1 investigator-initiated trial for cancer in combination with immunotherapy, alongside earlier-stage assets including CRO-67 (Chroma™ platform, pancreatic cancer preclinical) and SOF-VAC (Sofra™ platform, mRNA vaccine safety/efficacy improvement). Noxopharm is pre-revenue with no marketed products; its economic model is structured around a dual-track strategy of developing selected compounds in-house while pursuing external commercial arrangements (out-licensing, co-development, and partnerships with pharmaceutical companies) for other assets. The corporate group comprises Noxopharm Limited as the listed parent and wholly-owned subsidiary Pharmorage Pty Limited (a drug delivery/formulation entity). Recent strategic milestones include the granting of US patent protection for the Sofra™ platform in October 2025 and the May 2026 disclosure of new TLR8 amplification data, signalling continued platform validation and US-market intent.

Short descriptiontext

Noxopharm Limited (ASX:NOX) is an Australian clinical-stage biotech developing oligonucleotide (Sofra™) and small-molecule (Chroma™) drug candidates for cancer, autoimmune/inflammatory disease, and mRNA vaccine enhancement, with lead asset Veyonda® in Phase 1 oncology trials.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersTurramurra, Australia
HQ citystring
Turramurra
HQ countrystring
Australia
HQ regionstring
Oceania
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical stage drug development, immuno-oncology therapeutics, oligonucleotide based therapies, small molecule oncology, mRNA vaccine enhancement
Industry4 codes
1RNA Therapeutics Platforms & Design (sequence design, target ID/validation, AI/bioinformatics)
CodeHLAAADAGPrimaryYes
2Immuno-Oncology & Immune Monitoring Biomarkers (TMB, MSI, MRD, immune profiling)
CodeHLAAAMAKPrimaryNo
3Oncology Diagnostics (tumor profiling, MRD, liquid biopsy)
CodeHLAAALAEPrimaryNo
4Antisense Oligonucleotides (ASO) Therapeutics (splice modulation/knockdown)
CodeHLAAADACPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Pharmaceutical Preparation Manufacturing325412
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Clinical-stage biopharmaceutical drug development
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Pre-revenue R&D / future licensing
TypeLicensing Royalties
Description

Noxopharm is a clinical-stage biotech with no products on the market and therefore no product revenue. The company's economic model relies on capital raises (as an ASX-listed entity) and is structured around developing a pipeline of proprietary drugs across multiple platforms, with the explicit intent to develop certain compounds in-house while pursuing external commercial arrangements (licensing/out-licensing deals, co-development) for others. Future revenue is expected to be derived from licensing royalties, milestone payments, and eventual drug sales once candidates (Veyonda®, CRO-67, SOF-VAC) reach market.

noxopharm.com
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1Sofra™
Description

Technology platform with a pipeline of new proprietary drugs based on oligonucleotides (short strands of DNA/RNA building blocks), focused on mRNA vaccines and therapeutics, autoimmune disease and immuno-oncology.

noxopharm.com
+2 more records
Core offering1 text field

Noxopharm is a clinical-stage Australian biotech that develops novel drug candidates for cancer and inflammation through two proprietary technology platforms: Sofra™, an oligonucleotide-based platform that amplifies Toll-like receptor 8 (TLR8) activity for immuno-oncology, autoimmune/inflammatory disease, and mRNA vaccine enhancement, and Chroma™, a small-molecule oncology platform producing candidates such as preclinical CRO-67 for pancreatic cancer. Its lead clinical asset Veyonda® is currently being evaluated in a Phase 1 investigator-initiated trial for cancer in combination with immunotherapy, while the SOF-VAC program applies the Sofra™ platform to improve the safety profile of mRNA vaccines and therapeutics.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Noxopharm Limited (ASX:NOX) is a clinical-stage Australian biotech company built on a multi-platform architecture rather than a single unified product. Its portfolio is anchored by two proprietary technology platforms — Sofra™, an oligonucleotide-based platform (short nucleic acid sequences) targeting inflammation, autoimmunity, mRNA drug enhancement and immuno-oncology (including TLR8-amplifying compounds), and Chroma™, a small-molecule platform driving multiple cancer drug candidates. On top of these platforms sits Veyonda®, the company's lead clinical drug candidate currently in a Phase 1 investigator-initiated trial for cancer in combination with immunotherapy, while preclinical assets such as CRO-67 (from Chroma™, focused on pancreatic cancer) and application modules like SOF-VAC (mRNA vaccine improvement under Sofra™) extend the pipeline across cancer and inflammatory disease indications.

Product and service5 records
1Sofra™
CategoryTechnology platform
Description

Sofra™ is an oligonucleotide-based technology platform using short nucleic acid sequences that amplifies Toll-like receptor 8 (TLR8) activity, with applications spanning mRNA vaccine enhancement, autoimmune and inflammatory disease treatment, and immuno-oncology. It serves as the foundation for a pipeline of new proprietary drug candidates and is supported by granted US patent protection.

2Chroma™
CategoryTechnology platform
Description

Chroma™ is a small-molecule technology platform focused on developing multiple drug candidates primarily for cancer treatment, with leading preclinical candidate CRO-67 showing promising signals for the treatment of pancreatic cancer.

3Veyonda®
CategoryClinical drug candidate
Description

Veyonda® is Noxopharm's clinical-stage drug candidate currently in a Phase 1 investigator-initiated clinical trial for the treatment of cancer in combination with immunotherapy.

4CRO-67
CategoryPreclinical drug candidate
Description

CRO-67 is the leading preclinical drug candidate from Noxopharm's Chroma™ small-molecule platform, showing promising signals for the treatment of pancreatic cancer.

5SOF-VAC
CategoryApplication program
Description

SOF-VAC is an application program of the Sofra™ platform aimed at improving the safety profile and effectiveness of mRNA vaccines and therapeutics by reducing side effects and enhancing safety.

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
1Pharmorage Pty Limited
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Pharmorage Pty Limited (ACN 641 047 403) is listed as part of the Noxopharm Group of companies in Noxopharm's Privacy Policy and is featured as a dedicated page under the About Us section of the company's website. The Privacy Policy expressly states that the policy applies to each company in the Noxopharm Group, indicating Pharmorage is a related corporate entity operating within the same group structure.

noxopharm.com
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage UK biotech developing RNA-based therapeutics that engage innate immune pathways, including TLR8 agonism in oncology. Directly comparable to Noxopharm's Sofra™ platform as one of the few companies publicly pursuing oligonucleotide-based TLR8 immuno-oncology strategies.

TypeDirect peer
Description

Australian (ASX-listed) clinical-stage immuno-oncology company with a pipeline of B-cell vaccines, oncolytic viruses, and combination immunotherapies. Most directly comparable ASX peer in terms of size, stage, and immuno-oncology focus, allowing direct read-across on clinical and capital-markets dynamics.

TypeEmerging player
Description

Clinical-stage immuno-oncology company using computational discovery to identify novel drug targets and develop antibody-based therapeutics. Comparable in therapeutic area and stage, and provides a useful read-across for AI-driven target discovery applied to immune checkpoints and tumour microenvironment.

TypeBroad incumbent
Description

Global leader in mRNA therapeutics and vaccines with deep immuno-oncology pipeline. Relevant as a broad incumbent for the SOF-VAC mRNA-vaccine enhancement opportunity and as a benchmark for valuation of immuno-oncology platforms at scale.

TypeEmerging player
Description

Clinical-stage mRNA medicines company with self-amplifying RNA technology and partnerships in vaccines and rare disease. Comparable as a smaller, technology-focused mRNA company that partners with larger pharma, mirroring the out-licensing model Noxopharm intends to use for SOF-VAC.

TypeEmerging player
Description

US clinical-stage biotech developing tumour-activated immune-stimulating prodrugs (PREDATOR platform) for immuno-oncology. Comparable as an early-stage company engineering conditional immune activation in the tumour microenvironment, similar in spirit to Noxopharm's combination-immunotherapy positioning.

TypeRegional player
Description

Australian (ASX-listed) commercial-stage biopharmaceutical company developing diagnostic and therapeutic radiopharmaceuticals for cancer. Comparable as a successful Australian oncology biotech but at a much later commercial stage; provides relevant comparables on Australian biotech valuation and capital-markets access.

TypeDirect peer
Description

US clinical-stage immuno-oncology company developing immune-stimulating antibody conjugates that activate myeloid and antigen-presenting cells in the tumour microenvironment. Comparable to Noxopharm's ambition of combining tumour-targeting with immune activation, though using a different payload architecture.

TypeBroad incumbent
Description

Global mRNA platform company with commercial COVID-19 vaccine and an oncology pipeline. Provides relevant context for the mRNA-enhancement and oncology applications of Noxopharm's SOF-VAC program and for sizing the long-term opportunity if Sofra™ becomes a standard mRNA adjuvant.

TypeRegional player
Description

Australian (ASX-listed) clinical-stage biotech developing small-molecule oncology drugs, including for pancreatic cancer. Comparable as a domestic Australian clinical-stage peer with oncology focus, although the underlying mechanism (Chroma™ small molecules) is mechanistically distinct.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

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Headline, Details, Source

Competitive moat3 records

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Type, Details

Key risks5 records

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Key highlights5 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

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Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

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Compliance1 record

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Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors1 record

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Noxopharm

Clinical-stage biopharmaceutical drug developmentnoxopharm.com

Noxopharm Limited (ASX:NOX) is an Australian clinical-stage biotech developing oligonucleotide (Sofra™) and small-molecule (Chroma™) drug candidates for cancer, autoimmune/inflammatory disease, and mRNA vaccine enhancement, with lead asset Veyonda® in Phase 1 oncology trials.

What Noxopharm does

Noxopharm Limited (ASX:NOX) is an Australian clinical-stage biotechnology company founded in 2015 and headquartered in Castle Hill, NSW, developing novel therapeutics across oncology, autoimmune/inflammatory disease, and mRNA vaccine enhancement. The company operates two proprietary technology platforms: Sofra™, an oligonucleotide-based platform using short nucleic acid sequences to amplify Toll-like receptor 8 (TLR8) activity, which the company reports achieves more than 200-fold activity improvement over current best-in-class clinical comparators in human skin biopsies; and Chroma™, a small-molecule platform generating multiple oncology drug candidates, with leading preclinical asset CRO-67 positioned for pancreatic cancer.

The company's clinical pipeline centres on Veyonda®, which is in a Phase 1 investigator-initiated trial for cancer in combination with immunotherapy, alongside earlier-stage assets including CRO-67 (Chroma™ platform, pancreatic cancer preclinical) and SOF-VAC (Sofra™ platform, mRNA vaccine safety/efficacy improvement). Noxopharm is pre-revenue with no marketed products; its economic model is structured around a dual-track strategy of developing selected compounds in-house while pursuing external commercial arrangements (out-licensing, co-development, and partnerships with pharmaceutical companies) for other assets. The corporate group comprises Noxopharm Limited as the listed parent and wholly-owned subsidiary Pharmorage Pty Limited (a drug delivery/formulation entity). Recent strategic milestones include the granting of US patent protection for the Sofra™ platform in October 2025 and the May 2026 disclosure of new TLR8 amplification data, signalling continued platform validation and US-market intent.

Noxopharm firmographics

Firmographics
Name
Noxopharm
Legal name
Noxopharm Limited
Website
https://noxopharm.com
Company type
Public
Founded year
2015
Operating status
Operating
Headcount range
501–1,000 employees
Short description
Noxopharm Limited (ASX:NOX) is an Australian clinical-stage biotech developing oligonucleotide (Sofra™) and small-molecule (Chroma™) drug candidates for cancer, autoimmune/inflammatory disease, and mRNA vaccine enhancement, with lead asset Veyonda® in Phase 1 oncology trials.
Ownership category
akta.pro rank

Noxopharm industry classification

Industry
Product category
Clinical-stage biopharmaceutical drug development
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Pharmaceutical Preparation Manufacturing (325412)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
RNA Therapeutics Platforms & Design (sequence design, target ID/validation, AI/bioinformatics) (HLAAADAG)
akta.pro secondary industries
Immuno-Oncology & Immune Monitoring Biomarkers (TMB, MSI, MRD, immune profiling) (HLAAAMAK), Oncology Diagnostics (tumor profiling, MRD, liquid biopsy) (HLAAALAE), Antisense Oligonucleotides (ASO) Therapeutics (splice modulation/knockdown) (HLAAADAC)

Keywords

  • Clinical stage drug development
  • Immuno-oncology therapeutics
  • Oligonucleotide based therapies
  • Small molecule oncology
  • MRNA vaccine enhancement

Where Noxopharm is headquartered

Location

Headquarters

HQ city
Turramurra
HQ country
Australia
HQ region
Oceania

Offices1 record

Markets served

Noxopharm business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales, Others

Revenue model

  1. Pre-revenue R&D / future licensing: Noxopharm is a clinical-stage biotech with no products on the market and therefore no product revenue. The company's economic model relies on capital raises (as an ASX-listed entity) and is structured around developing a pipeline of proprietary drugs across multiple platforms, with the explicit intent to develop certain compounds in-house while pursuing external commercial arrangements (licensing/out-licensing deals, co-development) for others. Future revenue is expected to be derived from licensing royalties, milestone payments, and eventual drug sales once candidates (Veyonda®, CRO-67, SOF-VAC) reach market.

Go-to-market motion2 records

Distribution channels2 records

Marketing channels7 records

Noxopharm product offering

Product offering

Core offering

Noxopharm is a clinical-stage Australian biotech that develops novel drug candidates for cancer and inflammation through two proprietary technology platforms: Sofra™, an oligonucleotide-based platform that amplifies Toll-like receptor 8 (TLR8) activity for immuno-oncology, autoimmune/inflammatory disease, and mRNA vaccine enhancement, and Chroma™, a small-molecule oncology platform producing candidates such as preclinical CRO-67 for pancreatic cancer. Its lead clinical asset Veyonda® is currently being evaluated in a Phase 1 investigator-initiated trial for cancer in combination with immunotherapy, while the SOF-VAC program applies the Sofra™ platform to improve the safety profile of mRNA vaccines and therapeutics.

Product overview

Noxopharm Limited (ASX:NOX) is a clinical-stage Australian biotech company built on a multi-platform architecture rather than a single unified product. Its portfolio is anchored by two proprietary technology platforms — Sofra™, an oligonucleotide-based platform (short nucleic acid sequences) targeting inflammation, autoimmunity, mRNA drug enhancement and immuno-oncology (including TLR8-amplifying compounds), and Chroma™, a small-molecule platform driving multiple cancer drug candidates. On top of these platforms sits Veyonda®, the company's lead clinical drug candidate currently in a Phase 1 investigator-initiated trial for cancer in combination with immunotherapy, while preclinical assets such as CRO-67 (from Chroma™, focused on pancreatic cancer) and application modules like SOF-VAC (mRNA vaccine improvement under Sofra™) extend the pipeline across cancer and inflammatory disease indications.

Differentiator

Problem solved

Functional benefit

Brands

  • Sofra™: Technology platform with a pipeline of new proprietary drugs based on oligonucleotides (short strands of DNA/RNA building blocks), focused on mRNA vaccines and therapeutics, autoimmune disease and immuno-oncology.
  • Chroma™
  • Veyonda®

Products and services

  • Sofra™ Sofra™ is an oligonucleotide-based technology platform using short nucleic acid sequences that amplifies Toll-like receptor 8 (TLR8) activity, with applications spanning mRNA vaccine enhancement, autoimmune and inflammatory disease treatment, and immuno-oncology. It serves as the foundation for a pipeline of new proprietary drug candidates and is supported by granted US patent protection.
  • Chroma™ Chroma™ is a small-molecule technology platform focused on developing multiple drug candidates primarily for cancer treatment, with leading preclinical candidate CRO-67 showing promising signals for the treatment of pancreatic cancer.
  • Veyonda® Veyonda® is Noxopharm's clinical-stage drug candidate currently in a Phase 1 investigator-initiated clinical trial for the treatment of cancer in combination with immunotherapy.
  • CRO-67 CRO-67 is the leading preclinical drug candidate from Noxopharm's Chroma™ small-molecule platform, showing promising signals for the treatment of pancreatic cancer.
  • SOF-VAC SOF-VAC is an application program of the Sofra™ platform aimed at improving the safety profile and effectiveness of mRNA vaccines and therapeutics by reducing side effects and enhancing safety.

Companies that use Noxopharm

Customer profile

Segments3 records

Ideal customer profiles3 records

Noxopharm technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Noxopharm partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Pharmorage Pty LimitedcoreStrategic or Co-development PartnerPharmorage Pty Limited (ACN 641 047 403) is listed as part of the Noxopharm Group of companies in Noxopharm's Privacy Policy and is featured as a dedicated page under the About Us section of the company's website. The Privacy Policy expressly states that the policy applies to each company in the Noxopharm Group, indicating Pharmorage is a related corporate entity operating within the same group structure.

Scale indicators5 records

Recent moves6 records

Expansion highlights5 records

Noxopharm competitors and assessment

Company assessment

Direct peers

  • MiNA Therapeutics: Clinical-stage UK biotech developing RNA-based therapeutics that engage innate immune pathways, including TLR8 agonism in oncology. Directly comparable to Noxopharm's Sofra™ platform as one of the few companies publicly pursuing oligonucleotide-based TLR8 immuno-oncology strategies.
  • Imugene: Australian (ASX-listed) clinical-stage immuno-oncology company with a pipeline of B-cell vaccines, oncolytic viruses, and combination immunotherapies. Most directly comparable ASX peer in terms of size, stage, and immuno-oncology focus, allowing direct read-across on clinical and capital-markets dynamics.
  • Bolt Biotherapeutics: US clinical-stage immuno-oncology company developing immune-stimulating antibody conjugates that activate myeloid and antigen-presenting cells in the tumour microenvironment. Comparable to Noxopharm's ambition of combining tumour-targeting with immune activation, though using a different payload architecture.

Emerging players

  • Compugen: Clinical-stage immuno-oncology company using computational discovery to identify novel drug targets and develop antibody-based therapeutics. Comparable in therapeutic area and stage, and provides a useful read-across for AI-driven target discovery applied to immune checkpoints and tumour microenvironment.
  • Arcturus Therapeutics: Clinical-stage mRNA medicines company with self-amplifying RNA technology and partnerships in vaccines and rare disease. Comparable as a smaller, technology-focused mRNA company that partners with larger pharma, mirroring the out-licensing model Noxopharm intends to use for SOF-VAC.
  • Werewolf Therapeutics: US clinical-stage biotech developing tumour-activated immune-stimulating prodrugs (PREDATOR platform) for immuno-oncology. Comparable as an early-stage company engineering conditional immune activation in the tumour microenvironment, similar in spirit to Noxopharm's combination-immunotherapy positioning.

Broad incumbents

  • BioNTech: Global leader in mRNA therapeutics and vaccines with deep immuno-oncology pipeline. Relevant as a broad incumbent for the SOF-VAC mRNA-vaccine enhancement opportunity and as a benchmark for valuation of immuno-oncology platforms at scale.
  • Moderna: Global mRNA platform company with commercial COVID-19 vaccine and an oncology pipeline. Provides relevant context for the mRNA-enhancement and oncology applications of Noxopharm's SOF-VAC program and for sizing the long-term opportunity if Sofra™ becomes a standard mRNA adjuvant.

Regional players

  • Telix Pharmaceuticals: Australian (ASX-listed) commercial-stage biopharmaceutical company developing diagnostic and therapeutic radiopharmaceuticals for cancer. Comparable as a successful Australian oncology biotech but at a much later commercial stage; provides relevant comparables on Australian biotech valuation and capital-markets access.
  • PharmAust: Australian (ASX-listed) clinical-stage biotech developing small-molecule oncology drugs, including for pancreatic cancer. Comparable as a domestic Australian clinical-stage peer with oncology focus, although the underlying mechanism (Chroma™ small molecules) is mechanistically distinct.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat3 records

Key risks5 records

Key highlights5 records

Customer concentration

Noxopharm social profiles

Digital presence

Noxopharm compliance and trust

Trust signal

Compliance1 record

Noxopharm financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Noxopharm leadership team

Management profile

Number of profiles

Profiles1 record

Noxopharm subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Noxopharm funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors1 record

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Noxopharm M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Noxopharm

What does Noxopharm do?

Noxopharm is a clinical-stage Australian biotech that develops novel drug candidates for cancer and inflammation through two proprietary technology platforms: Sofra™, an oligonucleotide-based platform that amplifies Toll-like receptor 8 (TLR8) activity for immuno-oncology, autoimmune/inflammatory disease, and mRNA vaccine enhancement, and Chroma™, a small-molecule oncology platform producing candidates such as preclinical CRO-67 for pancreatic cancer. Its lead clinical asset Veyonda® is currently being evaluated in a Phase 1 investigator-initiated trial for cancer in combination with immunotherapy, while the SOF-VAC program applies the Sofra™ platform to improve the safety profile of mRNA vaccines and therapeutics.

Is Noxopharm a public or private company?

Noxopharm is a public company. It is classified as public and is currently operating.

When was Noxopharm founded?

Noxopharm was founded in 2015. It employs 501 to 1,000 people.

Where is Noxopharm based?

Noxopharm is headquartered in Turramurra, Australia, in the Oceania region.

How does Noxopharm make money?

One revenue line is on record: pre-revenue R&D / future licensing.

Who are Noxopharm's main competitors?

Direct peers on record are MiNA Therapeutics, Imugene and Bolt Biotherapeutics. Emerging players are Compugen, Arcturus Therapeutics and Werewolf Therapeutics. Broad incumbents are BioNTech and Moderna. Regional players are Telix Pharmaceuticals and PharmAust.

Does Noxopharm have an API?

No public API is recorded for Noxopharm.

What industry is Noxopharm in?

Noxopharm's product category is Clinical-stage biopharmaceutical drug development. Its primary akta.pro industry code is HLAAADAG, RNA Therapeutics Platforms & Design (sequence design, target ID/validation, AI/bioinformatics), with a secondary code of HLAAAMAK, Immuno-Oncology & Immune Monitoring Biomarkers (TMB, MSI, MRD, immune profiling). Its NAICS code is 541714 and its SIC code is 2834.

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Live signals
TradingViewPreclinical Data Shows Noxopharm’s Sofra Technology Can Enhance Current Cancer TreatmentsNoxopharm reported preclinical data showing its Sofra technology amplifies TLR8 activity, enhancing immune response to dying cancer cells. The data, from a study with Hudson Institute, showed significant immune activation when the oligonucleotide was combined with dying cancer cells. The company is scaling up to test compounds in humanised TLR8 mice and cancer models.Small CapsNoxopharm Studies Confirm Cancer-Fighting Potential of Sofra PlatformClinical-stage biotech company Noxopharm has announced new research data demonstrating that its Sofra technology platform, based on short nucleic acid sequences, can amplify toll-like receptor 8 (TLR8) activity by more than 200-fold in human skin biopsies and nearly three-fold in animal models. The platform, which received US patent protection in October, is being positioned as a potential new treatment modality in immuno-oncology that could enhance the cancer-fighting activity of standard therapies such as chemotherapy and radiotherapy. The company is now scaling up to test the novel compounds in humanized TLR8 mice and various cancer models.Biotech DispatchNew data confirms cancer-fighting potential of Sofra technology platformNoxopharm announced new data demonstrating the cancer-fighting potential of its Sofra technology platform, which uses oligonucleotides to amplify Toll-like receptor 8 (TLR8) activity against cancer cells. The study showed that a proprietary TLR8-amplifying oligonucleotide boosted activity more than 200-fold in human skin biopsies compared to current best-in-class drugs in clinical development. CEO Dr Olivier Laczka stated the findings support a new approach to addressing unmet needs in cancer treatment and could pave the way for a potentially disruptive new treatment modality.GlobeNewswirePositive DARRT-1 Data in Late-Stage Prostate CancerNoxopharm reported positive end-of-study data from its DARRT-1 Phase 1b trial, where 10 of 15 patients (66%) had stable disease or better at 6 months. The combination of Veyonda and palliative radiotherapy also reduced pain in 62% of patients. The company plans a pivotal DARRT-2/DARRT-3 study starting in 2020.GlobeNewswireNoxopharm Announces Appointment of Chief Commercial OfficerNoxopharm appointed Alexander Hunter as Chief Commercial Officer, bringing 15 years of corporate finance and growth company experience. He previously led an ASX listed energy company that grew revenue to over $200m and raised over $300m. The appointment supports Noxopharm's planned dual listing in 2020 and expanded clinical program for Veyonda.GlobeNewswirePotential for Fundamental Change in the Treatment of Brain CancerNoxopharm announced a research program using glutamate-inhibition technology to treat glioblastoma multiforme (GBM), citing recent research on glutamate's role in GBM growth. The company has lead candidates from a 2016 collaboration with UNSW Sydney, and the program is secondary to its Veyonda prostate cancer program.GlobeNewswireFurther Data Review Shows Major Clinical Benefits From Veyonda®Noxopharm announced that Veyonda, a suppository drug, significantly boosts the effectiveness of 177Lu-PSMA radiation therapy in advanced prostate cancer. The data shows PSA response doubled, progression-free survival quadrupled, and treatment duration tripled. Noxopharm expects Veyonda to become a standard companion drug for this therapy.GlobeNewswireVeyonda® and Radiotherapy Profiled at Key Oncology MeetingNoxopharm will present Veyonda research at the COSA oncology meeting in November, including DARRT-1 interim data showing a durable anti-cancer response at 6 months. An investigator-led LuPIN study also shows Veyonda significantly improves response to 177lutetium-PSMA-617. Both studies continue with final results expected in late 2020.GlobeNewswirePromising Data Leads to Expansion of LuPIN TrialNoxopharm expanded the LuPIN trial to add 24 patients on Veyonda 1200 mg daily with 177Lu-PSMA-617, based on encouraging results from 32 patients. The expansion aims to test dose-response effects, with 56 patients total expected to lay the foundation for a pivotal Phase II/III registration trial.GlobeNewswireLuPIN Trial Demonstrates High Rates of ResponseNoxopharm announced interim results from the LuPIN trial, a dose-finding study of Veyonda with 177Lu-PSMA-617 in metastatic castration-resistant prostate cancer. The 69% combined PSA response rate, with 75% in the 800mg cohort, exceeds rates seen with 177Lu-PSMA-617 alone. The company awaits results from the next 16 patients in the 800mg dose expansion cohort.